Allele Registry

Canonical Allele Identifier: PA095733

Gene: GCDH HGNC NCBI

ClinVar RCV:

RCV000002162

RCV000724276

ClinVar Variation:

2081

HGVS (amino-acid)	Matching Registered Transcripts
NP_000150.1:p.Tyr295His	CA252094 NM_000159.4:c.883T>C